RS138855624 VARS2

Health Risk Chr 6:30924437 snv missense variant
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Associated Conditions
Combined oxidative phosphorylation defect type 20
Combined oxidative phosphorylation defect type 20
Population Frequencies
gnomAD ALL
100%
1kG AFR
99.3%
1kG ALL
99.8%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
99.7%
Other Variants in VARS2
rs587777583 rs587777584 rs587777585 rs139515727 rs775439829 rs1554268077 rs200168128 rs367960344 rs202201763 rs778868393
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